Indications
Repatha® is indicated:
  • In adults with established cardiovascular disease to reduce the risk of myocardial infarction, stroke, and coronary revascularization
  • As an adjunct to diet, alone or in combination with other low-density lipoprotein cholesterol (LDL-C)-lowering therapies, in adults with primary hyperlipidemia, including heterozygous familial hypercholesterolemia (HeFH) to reduce LDL-C

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Please note: This form is intended for US healthcare professionals only.

If you are a Repatha® patient, please visit RepathaReady® or call 1-844-REPATHA for support.

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Whether you have product-related questions or need Repatha® samples, Repatha® Sales Representatives are here to help you and your office staff.

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To report an adverse event, please call 1-800-77-AMGEN (1-800-772-6436).

Privacy Statement
By clicking "Submit," you agree to disclose your personal information to Amgen and to be contacted by Amgen and their agents in the future regarding products, services, and/or information related to Repatha®. For more information about Amgen's privacy practices, please visit www.amgen.com/privacy.

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COVERAGE INFORMATION

Your patients count on you. You can count on us

Now, more than 80%* of prescriptions for Repatha® patients cost less than $50 per month1,*


89% of prescriptions cost patients less than $50

Discover the Repatha® Copay Card


100% of prescriptions cost patients less than $50 with most patients paying less than $10



72% of prescriptions cost patients less than $50

Learn about the LIS "Extra Help" program below


*Based on IQVIA claims data from 01/2020 through 12/2020 using commercial, health exchange, Medicare and Medicaid claims.

Percentage is based upon claims data including those where copay card was used.

Patient out-of-pocket costs can vary throughout the year depending on which phase of the Part D benefit they are currently in. Medicare Part D drug coverage is divided into 4 phases, each with a different cost-sharing amount. Those phases are 1) Deductible, 2) Initial coverage, 3) Coverage gap, 4) Catastrophic.

A REPATHA® ACCESS SPECIALIST (OR RAS)

provides access education and support to offices in order to help Repatha® patients access their therapy.

AREAS OF FOCUS

  • Prior authorizations/reauthorizations
  • Appeals process
  • Insurance information/utilization management (UM) criteria
  • Financial support resources
  • General access information/education
  • Help is available in person or virtually

Speak to your Repatha® representative to obtain your RAS contact information. You can reach out to your RAS for help with any of the above.

Repatha® Copay Card reduces costs for Repatha® for eligible commercially insured patients.

CoverMyMeds®: offers electronic prior authorization submission


CoverMyMeds® electronically connects providers, pharmacists, and health plans


  • Offers a process for submitting electronic prior authorizations (ePAs) for Repatha®
  • Live chat and phone support available
  • The ability to attach documentation if required

Visit CoverMyMeds to learn more.



CoverMyMeds Brochure


Learn more details about the CoverMyMeds Program in this brochure


Download

Full LIS Medicare patients pay no more than $10.35 per Repatha® prescription


The LIS program, also known as “Extra Help,” limits prescription out-of-pocket costs for eligible Medicare Part D patients with limited income and resource limits.

Learn more about LIS or call 1-844-REPATHA.


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Safety Net Foundation


Serving patients in need™

The Amgen Safety Net Foundation (ASNF) helps patients with financial need gain access to Amgen medicines at no cost.

Click here to see if your patient is eligible.

LIS = low-income subsidy.

Reference: 1. Data on file, Amgen; 2021.

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CVD = cardiovascular disease; LDL-C = low-density lipoprotein cholesterol; MI = myocardial infarction.

LDL-C = low-density lipoprotein cholesterol; MI = myocardial infarction.

ACS = acute coronary syndrome; LDL-C = low-density lipoprotein cholesterol; MI = myocardial infarction; PCSK9 = proprotein convertase subtilisin/kexin type 9.

Reference: 1. Repatha® (evolocumab) prescribing information, Amgen.


INDICATIONSRepatha® is indicated:
  • In adults with established cardiovascular disease to reduce the risk of myocardial infarction, stroke, and coronary revascularization
  • As an adjunct to diet, alone or in combination with other low-density lipoprotein cholesterol (LDL-C)-lowering therapies, in adults with primary hyperlipidemia, including heterozygous familial hypercholesterolemia (HeFH) to reduce LDL-C
IMPORTANT SAFETY INFORMATION

Contraindication: Repatha® is contraindicated in patients with a history of a serious hypersensitivity reaction to evolocumab or any of the excipients in Repatha®. Serious hypersensitivity reactions including angioedema have occurred in patients treated with Repatha®.

Hypersensitivity Reactions: Hypersensitivity reactions, including angioedema, have been reported in patients treated with Repatha®. If signs or symptoms of serious hypersensitivity reactions occur, discontinue treatment with Repatha®, treat according to the standard of care, and monitor until signs and symptoms resolve.

Adverse Reactions in Primary Hyperlipidemia: The most common adverse reactions (>5% of patients treated with Repatha® and more frequently than placebo) were: nasopharyngitis, upper respiratory tract infection, influenza, back pain, and injection site reactions.

From a pool of the 52-week trial and seven 12-week trials: Local injection site reactions occurred in 3.2% and 3.0% of Repatha®-treated and placebo-treated patients, respectively. The most common injection site reactions were erythema, pain, and bruising. Hypersensitivity reactions occurred in 5.1% and 4.7% of Repatha®-treated and placebo-treated patients, respectively. The most common hypersensitivity reactions were rash (1.0% versus 0.5% for Repatha® and placebo, respectively), eczema (0.4% versus 0.2%), erythema (0.4% versus 0.2%), and urticaria (0.4% versus 0.1%).

Adverse Reactions in the Cardiovascular Outcomes Trial: The most common adverse reactions (>5% of patients treated with Repatha® and more frequently than placebo) were: diabetes mellitus (8.8% Repatha®, 8.2% placebo), nasopharyngitis (7.8% Repatha®, 7.4% placebo), and upper respiratory tract infection (5.1% Repatha®, 4.8% placebo).

Among the 16,676 patients without diabetes mellitus at baseline, the incidence of new-onset diabetes mellitus during the trial was 8.1% in patients treated with Repatha® compared with 7.7% in patients that received placebo.

Immunogenicity: Repatha® is a human monoclonal antibody. As with all therapeutic proteins, there is potential for immunogenicity with Repatha®.

Please see full Prescribing Information.

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IMPORTANT SAFETY INFORMATION

Contraindication: Repatha® is contraindicated in patients with a history of a serious hypersensitivity reaction to evolocumab or any of the excipients in Repatha®. Serious hypersensitivity reactions including angioedema have occurred in patients treated with Repatha®.

Hypersensitivity Reactions: Hypersensitivity reactions, including angioedema, have been reported in patients treated with Repatha®. If signs or symptoms of serious hypersensitivity reactions occur, discontinue treatment with Repatha®, treat according to the standard of care, and monitor until signs and symptoms resolve.

Adverse Reactions in Primary Hyperlipidemia: The most common adverse reactions (>5% of patients treated with Repatha® and more frequently than placebo) were: nasopharyngitis, upper respiratory tract infection, influenza, back pain, and injection site reactions.

From a pool of the 52-week trial and seven 12-week trials: Local injection site reactions occurred in 3.2% and 3.0% of Repatha®-treated and placebo-treated patients, respectively. The most common injection site reactions were erythema, pain, and bruising. Hypersensitivity reactions occurred in 5.1% and 4.7% of Repatha®-treated and placebo-treated patients, respectively. The most common hypersensitivity reactions were rash (1.0% versus 0.5% for Repatha® and placebo, respectively), eczema (0.4% versus 0.2%), erythema (0.4% versus 0.2%), and urticaria (0.4% versus 0.1%).

Adverse Reactions in the Cardiovascular Outcomes Trial: The most common adverse reactions (>5% of patients treated with Repatha® and more frequently than placebo) were: diabetes mellitus (8.8% Repatha®, 8.2% placebo), nasopharyngitis (7.8% Repatha®, 7.4% placebo), and upper respiratory tract infection (5.1% Repatha®, 4.8% placebo).

Among the 16,676 patients without diabetes mellitus at baseline, the incidence of new-onset diabetes mellitus during the trial was 8.1% in patients treated with Repatha® compared with 7.7% in patients that received placebo.

Immunogenicity: Repatha® is a human monoclonal antibody. As with all therapeutic proteins, there is potential for immunogenicity with Repatha®.

Please see full Prescribing Information.